Advair and CHRONIC OBSTRUCTIVE PULMONARY DISEASE

481 reports of this reaction

2.4% of all Advair reports

#7 most reported adverse reaction

Overview

CHRONIC OBSTRUCTIVE PULMONARY DISEASE is the #7 most commonly reported adverse reaction for Advair, manufactured by GlaxoSmithKline LLC. There are 481 FDA adverse event reports linking Advair to CHRONIC OBSTRUCTIVE PULMONARY DISEASE. This represents approximately 2.4% of all 20,040 adverse event reports for this drug.

Patients taking Advair who experience chronic obstructive pulmonary disease should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.

Reporting Frequency

CHRONIC OBSTRUCTIVE PULMONARY DISEASE481 of 20,040 reports

CHRONIC OBSTRUCTIVE PULMONARY DISEASE is a less commonly reported adverse event for Advair, but still significant enough to appear in the safety profile.

Other Side Effects of Advair

In addition to chronic obstructive pulmonary disease, the following adverse reactions have been reported for Advair:

Frequently Asked Questions

Does Advair cause CHRONIC OBSTRUCTIVE PULMONARY DISEASE?

CHRONIC OBSTRUCTIVE PULMONARY DISEASE has been reported as an adverse event in 481 FDA reports for Advair. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is CHRONIC OBSTRUCTIVE PULMONARY DISEASE with Advair?

CHRONIC OBSTRUCTIVE PULMONARY DISEASE accounts for approximately 2.4% of all adverse event reports for Advair, making it a notable side effect.

What should I do if I experience CHRONIC OBSTRUCTIVE PULMONARY DISEASE while taking Advair?

If you experience chronic obstructive pulmonary disease while taking Advair, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.

Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.